Author

C. M. Overall

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 1 Cancer Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Assay:proteomics· 3 Research Focus:cancer & tumor microenvironment· 2 Research Focus:cell signaling & trafficking· 2 Research Focus:host-pathogen & immune response· 1 Organism:mouse· 1

Frequent Co-Authors

A. Kozik· 1 shared A. Lesner· 1 shared A. Mallavialle· 1 shared A. Pecak· 1 shared A. Pejkovska· 1 shared A. Wojtysiak· 1 shared B. N. Hay· 1 shared C. Dieryckx· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperBiochemistry

A. Kozik

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Cleavage of 14-3-3ϵ by the enteroviral 3C protease dampens RIG-I mediated antiviral signaling

D. D. Andrews, Y. Mohamud, M. Vlok, D. Akbari Bani, B. N. Hay, L. J. Foster, H. Luo, C. M. Overall, E. Jan

This study shows that enteroviral 3C protease cleaves 14-3-3ε, disrupting RIG-I signaling and promoting viral infection.

bioRxiv · Aug 31, 2022 · PreprintMicrobiology

A 9-kDa matricellular SPARC fragment released by cathepsin D exhibits pro-tumor activity in the triple-negative breast cancer microenvironment

L. B. Alcaraz, A. Mallavialle, T. David, D. Derocq, F. Delolme, C. Dieryckx, F. Boissiere-Michot, J. Simony-Lafontaine, S. Du Manoir, P. Huesgen, C. M. Overall, S. Tartare-Deckert, W. Jacot, T. Chardes, S. Guiu, , E. Liaudet-Coopman

The paper identifies a 9-kDa SPARC fragment released by cathepsin D in TNBC that promotes tumor progression by enhancing cell migration and invasion.

bioRxiv · Oct 22, 2020 · PreprintCancer Biology

Kallikrein-related peptidase 14 activates zymogens of membrane type matrix metalloproteinases (MT-MMPs) - a CleavEx library-based analysis

K. Falkowski, E. Bielecka, I. B. Thogersen, O. Bochenska, K. Płaza, M. Kalinska, L. Sasiadek, M. Magoch, A. Pecak, M. Wisniewska, N. Gruba, M. Wysocka, A. Wojtysiak, M. Brzezinska-Bodal, K. Sychowska, , T. Kantyka

This study identifies KLK14 as a specific activator of proMT-MMPs using a CleavEx library-based approach, revealing its role in ECM remodeling and potential implications in cancer.

bioRxiv · Apr 23, 2020Biochemistry